Overview

A Study of Budigalimab (ABBV-181) in Participants With Advanced Solid Tumors

Status:
Active, not recruiting
Trial end date:
2022-05-05
Target enrollment:
Participant gender:
Summary
This is an open-label, Phase I, dose-escalation study to determine the recommended Phase 2 dose (RPTD), maximum tolerated dose (MTD), and evaluate the safety and pharmacokinetic (PK) profile of budigalimab. This study will also evaluate the safety and tolerability of budigalimab in combination with Rovalpituzumab Tesirine and budigalimab in combination with venetoclax. The study will consist of 3 parts: budigalimab monotherapy dose escalation and expansion, budigalimab in combination with Rovalpituzumab Tesirine and budigalimab in combination with venetoclax.
Phase:
Phase 1
Details
Lead Sponsor:
AbbVie
Treatments:
Venetoclax